U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C6H10
Molecular Weight 82.1436
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,5-HEXADIENE

SMILES

C=CCCC=C

InChI

InChIKey=PYGSKMBEVAICCR-UHFFFAOYSA-N
InChI=1S/C6H10/c1-3-5-6-4-2/h3-4H,1-2,5-6H2

HIDE SMILES / InChI

Molecular Formula C6H10
Molecular Weight 82.1436
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Insight into the phase equilibrium phenomena of systems containing dienes and dicyanamide ionic liquids as a new potential application.
2010-12-02
(2SR,3SR)-Isopropyl 3-{[dimeth-yl(phenyl)-sil-yl]meth-yl}-2-hy-droxy-2-vinyl-pent-4-enoate.
2010-11-06
On the relationship between structure and reaction rate in olefin ring-closing metathesis.
2010-10-14
Metalla-cope rearrangements: bridging organic and inorganic chemistry.
2010-08-26
Cyclopolymerization of Nonconjugated Dienes with a Tridentate Phenoxyamine Hafnium Complex Supported by an sp(3) -C Donor: Isotactic Enchainment and Diastereoselective cis-Ring Closure.
2009-11-19
ESIMS studies and calculations on alkali-metal adduct ions of ruthenium olefin metathesis catalysts and their catalytic activity in metathesis reactions.
2009-10-19
Asymmetric Rh-catalyzed intermolecular hydroacylation of 1,5-hexadiene with salicylaldehyde.
2009-10
QTAIM study on the degenerate cope rearrangements of 1,5-hexadiene and semibullvalene.
2009-04-02
Synchrotron photoionization mass spectrometry measurements of kinetics and product formation in the allyl radical (H2CCHCH2) self-reaction.
2008-10-02
Structure-activity relationship (SAR) for the gas-phase ozonolysis of aliphatic alkenes and dialkenes.
2008-04-07
Structure and reaction mechanism of basil eugenol synthase.
2007-10-03
Calculational and experimental investigations of the pressure effects on radical-radical cross combination reactions: C2H5+C2H3.
2007-07-26
Allylic hydrogen abstraction II. H-abstraction from 1,4 type polyalkenes as a model for free radical trapping by polyunsaturated fatty acids (PUFAs).
2007-04-28
Studies of the electron-promoted cope cyclization of 2,5-phenyl-substituted 1,5-hexadiene radical anions.
2007-01-19
Diastereomerically-specific zirconium complexes of chiral salan ligands: isospecific polymerization of 1-hexene and 4-methyl-1-pentene and cyclopolymerization of 1,5-hexadiene.
2006-10-11
Primary mechanism of the thermal decomposition of tricyclodecane.
2006-10-05
One-pot synthesis of polysaccharide 3,5-dimethylphenylcarbamates having a random vinyl group for immobilization on silica gel as chiral stationary phases.
2006-07
Aquasonolysis of thioethers.
2006-05
Influence of vinyl monomers and temperature on immobilization of cellulose 3,5-dimethylphenylcarbamate onto silica gel as chiral stationary phases for high-performance liquid chromatography.
2006-02-03
A joint study based on the electron localization function and catastrophe theory of the chameleonic and centauric models for the Cope rearrangement of 1,5-hexadiene and its cyano derivatives.
2005-11-15
Balancing dynamic and nondynamic correlation for diradical and aromatic transition states: a renormalized coupled-cluster study of the cope rearrangement of 1,5-hexadiene.
2005-03-02
New ligand systems incorporating two and three 4,4'-bipyridine units. Characterization of bi- and trimetallic rhodium and iridium complexes.
2004-11-01
Hydrosilylation of dienes by yttrium hydrido complexes containing a linked amido-cyclopentadienyl ligand.
2004-08-07
Catalytic reduction of acetone by [(bpy)Rh]+: a theoretical mechanistic investigation and insight into cooperativity effects in this system.
2003-09-17
Dissociative and associative mechanisms of cope rearrangements of fluorinated 1,5-hexadienes and 2,2'-bis-methylenecyclopentanes.
2003-06-04
Double-chelation-assisted Rh-catalyzed intermolecular hydroacylation.
2003-04-17
Insertion/isomerization polymerization of 1,5-hexadiene: synthesis of functional propylene copolymers and block copolymers.
2002-10-02
Conformation-dependent state selectivity in O-O cleavage of ONOONO: an "inorganic cope rearrangement" helps explain the observed negative activation energy in the oxidation of nitric oxide by dioxygen.
2002-08-14
Convergent approach to pumiliotoxin alkaloids. Asymmetric total synthesis of (+)-pumiliotoxins A, B, and 225F.
2002-08-09
Synthesis of [n]- and [n.n]cyclophanes by using Suzuki-Miyaura coupling.
2002-07-26
Preparation and cell growth inhibitory activity of [PtR(2)L(2)] (R=polyfluorophenyl, L(2)=diene, cyclohexane-1,2-diamine (chxn) or cis-(dimethyl sulfoxide)(2)) and the X-ray crystal structure of [Pt(C(6)F(5))(2)(cis-chxn)].
2002-04-28
Cyclocopolymerization: a mechanistic probe for dual-site alternating copolymerization of ethylene and alpha-olefins.
2002-04-24
Transition-metal-promoted reactions of boron hydrides. 17. Titanium-catalyzed decaborane-olefin hydroborations.
2001-12-12
The structure of ionized 1,5 hexadiene in the gas phase.
2001-07
The effect of rigidity, shape, unsaturation, and length on the anesthetic potency of hydrocarbons.
2001-06
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:55:53 GMT 2025
Edited
by admin
on Mon Mar 31 18:55:53 GMT 2025
Record UNII
4MTZ4764FI
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1,5-HEXADIENE
Systematic Name English
NSC-60690
Preferred Name English
.ALPHA.,.OMEGA.-HEXADIENE
Common Name English
DIALLYL
Common Name English
BIALLYL
Common Name English
Code System Code Type Description
PUBCHEM
11598
Created by admin on Mon Mar 31 18:55:53 GMT 2025 , Edited by admin on Mon Mar 31 18:55:53 GMT 2025
PRIMARY
CAS
592-42-7
Created by admin on Mon Mar 31 18:55:53 GMT 2025 , Edited by admin on Mon Mar 31 18:55:53 GMT 2025
PRIMARY
NSC
60690
Created by admin on Mon Mar 31 18:55:53 GMT 2025 , Edited by admin on Mon Mar 31 18:55:53 GMT 2025
PRIMARY
FDA UNII
4MTZ4764FI
Created by admin on Mon Mar 31 18:55:53 GMT 2025 , Edited by admin on Mon Mar 31 18:55:53 GMT 2025
PRIMARY
MESH
C545783
Created by admin on Mon Mar 31 18:55:53 GMT 2025 , Edited by admin on Mon Mar 31 18:55:53 GMT 2025
PRIMARY
ECHA (EC/EINECS)
209-754-7
Created by admin on Mon Mar 31 18:55:53 GMT 2025 , Edited by admin on Mon Mar 31 18:55:53 GMT 2025
PRIMARY
WIKIPEDIA
1,5-Hexadiene
Created by admin on Mon Mar 31 18:55:53 GMT 2025 , Edited by admin on Mon Mar 31 18:55:53 GMT 2025
PRIMARY
EPA CompTox
DTXSID4049323
Created by admin on Mon Mar 31 18:55:53 GMT 2025 , Edited by admin on Mon Mar 31 18:55:53 GMT 2025
PRIMARY